AI Article Synopsis

  • Synthetic RNA systems outperform traditional protein networks with benefits like quicker responses, greater specificity, and the ability to be programmed for specific tasks.
  • The study introduces an RNA toggle switch that uses RNA aptamers to inhibit the activity of two RNA polymerases, T7 and SP6, with monitoring done via light-up aptamer systems.
  • The switch can alternate between two states by adding DNA sequences that bind to and block the inhibitory RNA aptamers, making it a potential tool for controlling nucleic acid networks in synthetic biology.

Article Abstract

Synthetic RNA systems offer unique advantages such as faster response, increased specificity, and programmability compared to conventional protein-based networks. Here, we demonstrate an RNA-based toggle switch using RNA aptamers capable of inhibiting the transcriptional activity of T7 or SP6 RNA polymerases. The activities of both polymerases are monitored simultaneously by using Broccoli and malachite green light-up aptamer systems. In our toggle switch, a T7 promoter drives the expression of SP6 inhibitory aptamers, and an SP6 promoter expresses T7 inhibitory aptamers. We show that the two distinct states originating from the mutual inhibition of aptamers can be toggled by adding DNA sequences to sequester the RNA inhibitory aptamers. Finally, we assessed our RNA-based toggle switch in degrading conditions by introducing controlled degradation of RNAs using a mix of RNases. Our results demonstrate that the RNA-based toggle switch could be used as a control element for nucleic acid networks in synthetic biology applications.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9007568PMC
http://dx.doi.org/10.1021/acssynbio.1c00580DOI Listing

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